An unusual arene oxide reaction. Solvent capture during acid

Oct 1, 1976 - An unusual arene oxide reaction. Solvent capture during acid-catalyzed solvolysis of 7,12-dimethylbenz[a]anthracene 5,6-oxide. John W. K...
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J.Org. Chem., Vol. 41, No. 21,1976 3487

Notes

We hope that this new synthetic procedure will stimulate interest i n cyanoformates. Experimental Section Many of these cyanoformates are known compounds; however, spectral properties even on those that are known are meager. For this reason, ir and NMR spectra of all compounds are reported here. The new cyanoformates, n-butyl, isobutyl, 2,2,2-trichloroethyl, and 2octyl, have been analyzed. Infrared spectra were obtained on a Perkin-Elmer 337 spectrometer and were calibrated against known bands in a polystyrene film. NMR spectra were recorded on a Varian T-60 spectrometer. Ten percent solutions in carbon tetrachloride with tetramethylsilane as internal standard were used. Vapor phase chromatography was carried out on a Hewlett-Packard F & M 700 using a 2090polyphenyl ether on Chromosorb P 4 ft X 0.25 in. column. Microanalysis was performed by Elek Microanalytical Laboratories, Torrance, Calif. Boiling points and melting points were not corrected. Preparation of Isobutyl Cyanoformate. In a 50-ml round-bottom flask equipped with a reflux condenser, nitrogen inlet, and a Tefloncovered magnetic stirring bar was placed 30 ml of methylene chloride, 3.5 g (0.054 mol) of potassium cyanide, 6.8 g (0.05 mol) of isobutyl chloroformate (Eastman), and approximately 50 mg (0.02 mmol) of 18-crown-6.18The mixture was stirred at room temperature. The reaction could be followed by ir (the disappearance of the band at 1790 cm-I due to the C=O of the starting chloroformate and the appearance of bands at 2250 cm-l due to the C=N and at 1750 cm-l due to the C=O of the product cyanoformate) or by GLC (the starting material had a shorter retention time than the product cyanoformate in all cases which were examined). When the starting material had disappeared (-4 h), the solution was filtered. The solution was distilled through a 15-cm Vigreux column. Solvent was removed at atmospheric pressure. A fraction consisting of pure isobutyl cyanoformate by GLC, 6.0 g (0.047 mol), 94%yield, distilled at 52-53 "C (20 mm): NMRd (2 H) 6 4.1, J = 7 Hz, m (1H) 2.1, d (6 H) 1.0,J = 7 Hz; ir 2250 C=N, and 1750 cm-l C=O. Anal. Calcd for CeH902N: C, 56.68; H, 7.14. Found: C, 56.70; H, 7.03. All other cyanoformates reported were prepared in analogous fashion. Methyl cyanoformate from methyl chloroformate (Aldrich): NMR s (3 H) 6 4.0; ir 2250 C=N, 1750 cm-' C=O. Ethyl cyanoformate from ethyl chloroformate (Aldrich): NMR q (2 H) 6 4.4, J == 7 Hz, t (3 H) 1.4,J = 7 Hz; ir 2250 C=N, and 1750 cm-1 C=O. n-Butyl cyanoformate from n-butyl chloroformate (Aldrich): NMR t (2 H) 6 4.4, J = 7 Hz, multiplets (7 H) 1.7-1.0; ir 2250 C=N, and 1750 cm-l C=O. Anal. Calcd for CeH902N: C, 56.68; H, 7.14. Found: C, 57.01; H, 7.10. 2,2,2-Trichloroethyl cyanoformate from 2,2,2-trichloroethyl chloroformate (Aldrich):NMR s (2 H) 6 4.75; ir 2250 C=N, and 1760 cm-l C=O. Anal. Calcd for C4HzOzNC13: C, 23.73; H, 1.00. Found: C, 23.87; H, 1.32. Isopropyl cyanoformate from isopropyl chloroformate (Research Organic/Inorganic Chemical Co.): NMR septet (1H) 6 5.2, J = 7 Hz, d (6 H) 1.4, J = 7 Hz; ir 2250 C=N, 1750 cm-' C=O. 2-Octyl cyanoformate from 2-octyl chloroformate which had been prepared by reaction of 2-octyl alcohol with phosgene:24NMR m (1 H) 6 5.1, m (16 €4') 1.3; ir 2250 C=N and 1745cm-l C=O. Anal. Calcd for C10H1702N: C, 65.54; H, 9.35. Found: C, 65.51; H, 9.31. Cyclohexyl cyanoformate from cyclohexyl chloroformate which had been prepared by reaction of cyclohexanol with phosgene:24NMR br (1H) 6 5.0, m (10 H) centered at 1.6; ir 2245 C=N, and 1745 cm-l

formate, 59873-33-5; 2-octyl chloroformate, 15586-11-5; cyclohexyl cyanoformate, 5532-84-4; cyclohexyl chloroformate, 13248-54-9; benzyl cyanoformate, 5532-86-5; benzyl chloroformate, 501-53-1; phenyl cyanoformate, 5532-82-1; phenyl chloroformate, 1885-14-9; potassium cyanide, 151-50-8.

References and Notes (1) E. S.Lewis and W. C. Herndon, J. Am. Chem. Soc., 83, 1955, 1959, 1961 (1961). (2) A. R. Choppin, H. A. Frediani, and G. F. Kirby Jr., J. Am. Chem. Soc., 81, 3176(1939). (3) A. R. Choppin and G. F. Kirby Jr., J. Am. Cbem. Soc., 62, 1592 (1940). (4) W. A. Sheppard, J. Org. Chem., 27, 3756 (1962). (5) T. Jaworski and B. Korybut-Daszkiewicz, Rocz. Chem., 41, 1521 (1967). (6) Y. Odaira, T. Shimodaira, and S. Tsutsumi, Chem. Commun., 757 (1967). (7) T. Tominaga, Y. Odaira, and S. Tsutsumi, Bull. Chem. Soc. Jpn., 37, 596 (1964). (8) Y. Shigemitsu, T. Tominaga, T. Shimodaira, Y. Odaira, and S. Tsutsumi, Bull. Chem. Soc. Jpn., 39, 2463 (1966). (9) L. A. Carpino, J. Org. Chem., 29, 2820 (1964). (IO) M. Leplawy and W. Stec, Bull. Acad. Pol. Sci., Ser. Scl. Chim., 12, 21 (1964). (11) 0. Achmatowicz, K. Beiniak, C. Borecki, and M. Leplawy, Rocz. Chem., 39, 1443 (1965). (12) W. J. Linn, "Oraanic Syntheses", Collect. Voi. V, Wiiey, New York, N.Y., 1973, p 1007. E. L. Martin, Org. Synth., 51, 70 (1971). W. Lidy and W. Sundermeyer, Tetrahedron Lett., 1449 (1973). E. C. Evers, W. 0. Freitag. J. N. Keith, W. A. Kriner, A. G. MacDiarmid,and S. Sujishi, J. Am. Chem. Soc., 81, 4493 (1959). D. A. Evans, G. L. Carroll, and L. K. Truesdale, J. Org. Chem., 39, 914 (1974). J. W. Zubrick, 6. I. Dunbar, and H. D. Durst, Tetrahedron Lett., 71 11975). (18) G.W.'Gokel, D. J. Cram, C. L. Liotta, H. P. Harris, and F. L. Cook, J. Org. Chm., 39, 2445 (1974). (19) C. L. Liotta and H. P. Harris, J. Am. Chem. Soc., 98, 2250 (1974). (20) C. L. Liotta, H. P. Harris, M. McDermott. T. Gonzalez,and K. Smith, Tetrahedron Lett., 2417 (1974). (21) H. D. Durst, TetrahedronLett.,2421 (1974). (22) K. E. Koenig and W. P. Weber, Tetrahedron Lett., 2275 (1974). (23) R. B. Woodward,K. Heusier,J. Gosteli,P. Naegelt,W. Oppolzer,R. Ramage. S. Ranganathan, and H. Vorbruggen, J. Am. Chem. Soc., 88, 852 (1966). (24) F. Strain,W. E. Bissinger,W. R. Dial, H. Rudoff, 8.J. DeWitt, H. C. Stevens, and J. H. Langston, J. Am. Cbem. Soc., 72, 1254 (1950).

An Unusual Arene Oxide Reaction. Solvent Capture during Acid-Catalyzed Solvolysis of 7,l%-Dimethylbenz[alanthracene 5,6-0xide John W. Keller, Nitya G. Kundu, and Charles Heidelberger*l McArdle Laboratory for Cancer Research, University of Wisconsin, Madison, Wisconsin 53706 Received April 16,1976 Recent interest in polycyclic arene oxides as mediators of polycyclic arene carcinogenesis2 has prompted us t o study the aqueous solvolysis of 7,12-dimethylbenz[a]anthracene5,6oxide ( l ) ,a K-region3 metabolite4 of t h e carcinogenic 7,12-

c=o.

-

Benzyl cyanoformate from benzyl chloroformate (Aldrich): NMR s (5 H)6 7.2, s (2 H) 5.0; ir 2245 C=N, and 1745 cm-l C=O.

water-

Phenyl cyanoformate from phenyl chloroformate (Eastman): NMR m (5 H) 6 7.3; ir 2250 C=N, and 1760 cm-l C=O.

Acknowledgments. This work was supported b y a grant from t h e National Science Foundation, GP-40331X. M. E. Childs thanks t h e Stauffer Chemical Co. for a fellowship. Registry No.-Isobutyl cyanoformate, 59873-30-2; isobutyl chloroformate, 543-27-1;methyl cyanoformate, 17640-15-2; methyl chloroformate, 79-22-1; ethyl cyanoformate, 623-49-4; ethyl chloroformate, 541-41-3; n-butyl cyanoformate, 5532-84-3; n-butyl chloroformate, 592-34-7; 2,2,2-trichloroethyl cyanoformate, 59873-31-3; 2,2,2-trichloroethyl chloroformate, 17341-93-4; isopropyl cyanoformate, 59873-32-4; isopropyl chloroformate, 108-23-6; 2-octyl cyano-

CH3

i

+

H: 37'

-2

3488 J.Org. Chem., Vol. 41, No. 21,1976

Notes

Table I. Product and Rate Data for t h e Reaction of 7,12Dimethylbenz[ alanthracene 5,6-0xide (1) in Acidic 1:l Dioxane-Water (v/v), 0.10 M in KCl at 36.8 "C Yieldb % Reaction PH" 1.0 3.0 5.0 5.50 5.90 6.20 6.60 7.0

hobsd X S-1

lo4,

22.2 12.4 5.67 2.44

+

5 6 Cis Trans ketones dihydrodiols dihvdrodiols 25 24 20 27 25

8 9 11 10 9

67 67 69 63 66

33 25

16 14

51 61

a By glass electrode. Integration of HPLC traces with correction for €264 values.

-7

,.I

Figure 1. Generation of a benzylic cation, 7, by reversible protonation of the oxirane oxygen followed by scission of the CS-0 bond.

(61, and is even lower than t h a t obtained from benz[a]anthracene 5,6-oxide (5) (Table 11).K-Region phenols, the major solvolysis product of the previously studied oxide^,^ could not be detected.

m@ H3cQg@ H2C-CH2'0 12 0

Table 11. Comparison of t h e Product and Rate Data on 7,12-Dimethylbenz[a]anthracene5,6-0xide with Related Benz[ alanthracene Oxides Not Containing Bay-Position Methyl Groups. Reactions Conducted in 1:l DioxaneWater 0.10 M in KCl at 37 "C Dihy- Cis/trans Reardrodiol ratio of rangeM-1 X yield, dihydro- ment lo-' % diols products kH,c

K-Region arene oxide BenzIaIanthracene 5,6-oxide (5)" 3-Methylcholanthrene 11,12-oxide(6)" 7,12-Dimethylbenz[alanthracene 5,6-oxide (1)b

1.5

25

31/69

Phenols

99

25

75/25

Phenols

90

75

15/85

Ketones

" Data from ref 5 . Data from this work. Specific acid catalyzed rate constant. dimethylbenz[a]anthracene.We report here t h a t in acidcatalyzed reactions, oxide 1 shows unusually high electrophilicity toward water, as compared t o several previously studied K-region arene oxidesS5Treatment of 1 with aqueous dioxane containing dilute acid produced mostly K-region dihydrodiols, 2, along with some K-region ketones, 3 and 4. In contrast, we previously found t h a t under the same conditions the K-region oxides of phenanthrene, benz[a]anthracene ( 5 ) , dibenz[a,h]anthracene, and 3-methylcholanthrene (6) all gave high yields of K-region phenols with lesser amounts of K-region d i h y d r o d i o l ~ . ~ Oxide 1 was maintained a t constant p H with dilute HCl in a p H stat a t 37 "C in 1:l dioxane-water (v/v), 0.10 M in KC1. After all the oxide had reacted, the products were analyzed by high-pressure liquid chromatography (HPLC). Eluted peaks were identified as K-region dihydrodiols, 2, and ketones, 3 and 4, by comparison of their retention volumes and ultraviolet spectra with those of authentic samples.69 HPLC of the ketones from reaction of oxide 1 a t p H 5.0 showed t h a t the 5 ketone, 3, and the 6 ketone, 4, were produced in t h e ratio of 2:3, respectively. Product yields as a function of p H are summarized in Table I. Control experiments showed t h a t under these reaction and analysis conditions the dihydrodiols are stable. The 75% yield of dihydrodiols is strikingly different from the 25% dihydrodiol yields we obtained from the reaction of several other arene oxide^.^ T h e cidtrans ratio of the dihydrodiols obtained from 1 was 15/85; this is much lower than that obtained from 3-methylcholanthrene 11,lZ-oxide

5

c

6

I

The kinetics of the solvolysis reaction a t 36.8 "C were monitored spectrophotometrically. The kobsd values for the first-order disappearance of oxide 1 are proportional to [H+] in the p H range 5-7 (Table I); the proportionality constant k~ is 900 M-l s-l. The pH-rate profile in this p H range is nearly identical with t h a t of 3-methylcholanthrene 11,12oxide (6),5910 and is consistent with reversible protonation of the oxirane oxygen, followed by rate-limiting ring opening t o Product an intermediate cation (for example, 7 in Figure l),5J1 formation then occurs rapidly either by attack of water or rearrangement, followed by proton loss. The formation of cations analogous to 7 from different arene oxides occurs a t different rates, according t o the ability of the attached aryl groups to stabilize the incipient positive charge a t the benzylic ~ a r b o nI.t~was shown in our previous work that there was a positive correlation between the k~ value for a given oxide and the cis/trans ratio of the product dihydrodiols.5 This is so because of the large amount of positive charge delocalized throughout t h e carbons of both the rate-limiting ring opening and the cis-addition transition states, whereas the positive charge density on the carbons of the trans-addition transition state is much 10wer.~Thus, solvolysis of 7,12-dimethylbenz[a]anthracene6-oxide (1) would, on electronic grounds, be expected t o produce nearly the same cis/ trans ratio as 6. In fact, however, the ratio from 1 is 15-fold lower. We have previously observed K-region dihydrodiols as products of acid-catalyzed solvolysis of arene oxides in 1:l dioxane-water, 0.10 M in KCl.5 In solvent water a t p H 6-7, phenanthrene 9,10-oxide and several alkylated benzene oxides also produce high yields of dihydrodiol.12J3 The trans dihydrodiol yields reported here, which are higher than we previously found,5 may be related t o the strain inherent in the 7,12-dimethylbenz[a]anthracene5,6-oxide system. Glusker et al.14 have shown by x-ray diffraction t h a t in the crystal, the phenyl ring of oxide 1 (carbon 1-4, l a , and 4a) is twisted such t h a t there is a dihedral angle of 28" between the phenyl and naphthyl rings (Figure 2). This twist may have two related effects: (1)it may cause the observed high rate of acid-catalyzed ring opening due to increased strain in the oxirane ring, and (2) it may largely prevent cis attack of water due to decreased conjugative interaction between the K-region carbons and the aryl moieties. The dihedral twist present in the ions from 1 may cause the observed low yield of rearrangement products by retarding the NIH shift,15 because the twist may inhibit full cyclic

J. Org. Chem., Vol. 41, No. 21,1976 3489

Notes

H

I-H +

c

H

7

w

Figure 2. Formation of cation 7 from the twisted arene oxide 1. conjugation in t h e N I H shift transition state? or cause t h e reacting C-H bond t o overlap less with t h e adjacent empty p orbital. The product ion of K-region ketones instead of phenols from solvolysis of 1 is a related phenomenon. Most arene oxides would be expected t o rearrange by the N I H shift t o ketones and rapidly tautomerize t o the more stable phenolic form.15 Phenols are usually more stable because the endocyclic double bond becomes delocalized as a result of conjugation with the neighboring aromatic groups.16However, in the case of 5- and 6-hydroxy-7,12-dimethylbenz[a]anthracenes, t h e noncoplanarity of the K-region endocyclic bond with the attached aryl groups should inhibit the full cyclic delocalization required for phenol ~ t a b i l i t y . ~Indeed, J~ it has been found t h a t t h e 5 and 6 ketones are more stable than the respective phenols, and t h a t the phenol-ketone tautomerization occurs only under conditions much more vigorous than we used (at 90 "C in 0.01 M HC1, t 1 / 2 = 10 h).8 Thus, ketones 3 and 4 are primary products of solvolysis that are formed by NIH shifts of cationic intermediates, but do not undergo the usual tautomerization because of steric destabilization of the phenols. In contrast, the phenols derived from rearrangement of benz[a]anthracene 5,6-oxide (5) and 3-methylcholanthrene Il,l2-oxide (6) are more stable than the respective ketones because the nearly planar aromatic ring s y s t e r n ~ ~allow ~ J ~delocalization of t h e endocyclic K-region double bonds. The foregoing results illustrate the profound effects which a substituent distal to t h e oxirane ring can have on t h e solvolytic reactivity of an arene oxide. However, the relationship of these r e s u h to the biological effects of 7,12-dimethylbenz[a]anthracene 5,6-oxide or its parent hydrocarbon remains to be determined.

Experimental Section Materials. Dioxane was purified by the method of Fieser.20It was mixed with an equal volume of double-distilled water, 0.200 M in KCl, sealed under nitrogen in 250-ml bottles, and stored at -20 "C. All other solvents were Spectrograde or were distilled before use. cis5,6-Dihydro-5,6~dihydroxy-7,12-dimethylbenz[u]-anthracene was synthesized by osmium tetroxide oxidation of the parent hydrocarbon;17 truns-5,6-dihydro-5,6-dihydroxy-7,12-dimethylbenz[u]anthracene was synthesized by lithium aluminum hydride reduction of the 5,6-quinone in ether followed by column chromatographic

separation (Florisil and benzene-ethanol) of the cis and trans dihydrodi01s.l~The oxide, 1, was synthesized by treatment of the trans dihydrodiol with dimethylformamide dimethyl acetal in benzene at reflux." The K-region ketones were synthesized by dehydration of the cis dihydrodiol in refluxing acetic acid-HC1, followed by Florisil-benzene column chromatography.8 Spectra. Uv spectra were recorded on a Cary 15 spectrophotometer. High-pressure Liquid Chromatography. A Du Pont Model 830 chromatograph equipped with a Zorbax (silica) column (0.25 m X 2.2 mm i.d.) and a 254-nm photometric detector was used. Elution of a reaction aliquot with 1:1 (v/v) hexane-(dichloromethane, 2-propanol, acetic acid; 100020:0.1) produced peaks at 8 ml (ketones 3 and 4),35 ml (cis dihydrodiol), and 80 ml (trans dihydrodiol). Integration was by multiplication of peak height by peak width at half height; a correction for the different e value at 254 nm was applied for the ketone Elution of a reaction aliquot with the upper layer of 25:1:0.2 (v/v) hexane-dioxane-formic acid produced peaks due to the 6 ketone, 4 (2.4 ml) and the 5 ketone, 3 (2.8 ml), in addition to the dihydrodiol peaks. Rate Measurements. Kinetics were performed similarly to previous experiments.j Reactions were run in a 20-ml stirred reactor thermostated at 36.8 f 0.05 "C and kept at constant pH by a Radiometer pH stat. Aliquots were removed by automatic pipet and immediately quenched in dioxane-water containing sodium bicarbonate. The absorbance of each quenched aliquot was read at 277.0 nm, a A,, of oxide 1; rate constants were obtained graphically from plots of In (At - A m ) vs. time.

Acknowledgments. This work was supported in part by Grants CA-07175 and CRTY-5002 from the National Cancer Institute, National Institutes of Health. Charles Heidelberger is a n American Cancer Society Professor of Oncology. Registry No.-l,39834-38-3; cis-2,2518-02-7;trans- 2,16644-15-8; 3.53306-07-3; 4,55327-65-6.

References and Notes LACIUSC Cancer Center,Los Angeles, Calif. 90033. P. L. Grover, P. Sims, E. Huberman, H. Marquardt, T. Kuroki, and C. Heidelberger, Proc. Natl. Acad. Sci. U.S.A., 68, 1098 (1971);H. Marquardt, T. Kuroki, E. Huberman, J. K. Selkirk, C. Heidelberger. P. L. Grover, and P. Sims, CancerRes., 32,716(1972);H. Marquardt, ibid., 34, 1612 (1974); H. Marquardt, J. E. Sodergren, P. Sims and P. L. Grover, lnt. J. Cancer, 13, 304 (1974).See also D. M. Jerina and J. W. Daly, Science, 185,573 (1974).

A. Pullman and B. Pullman, Adv. Cancer Res., 3, 117 (1955). G. R. Keysell, J. Booth, P. L. Grover, A. Hewer, and P. Sims. Biochem. fharmacol., 22,2853 (1973). J. W. Keller and C. Heidelberger, J. Am. Chem. Soc., 98,2328 (1976). J. W. Cook and R. Schoental,J. Chem. SOC.,170 (1948). P. Sims, Blochem. J., 98,215 (1966). A. Dipple, L. S. Levy, and P. T. lype, Cancer Res., 35,652 (1975). M. S.Newman and D. R. Olson, J. Am. Chem. Soc., 96,6207(1974).

Preliminary evidence indicates that oxide 1 also undergoes spontaneous solvolysis in 1:l dioxane-water, 0.10 M in KCi. (11) G. J. Kasparek, T. C.Bruice, H. Yagi and D. M.Jerina, J. Chem. Soc., Chem. Commun., 784 (1972). (12)G. J. Kasperek,T. C. Bruice, H. Yagi, N. Kaubisch, and D. M. Jerina, J. Am. Chem. SOC.,94,7876 (1972). (13)(a)P. Y. Bruice, T. C. Bruice. P. M. Dansette, H. G. Selander, H. Yagi, and D. M. Jerina, J. Am. Chem. Soc., g8, 2965 (1976).(b) P. Y. Bruice, T. C. Bruice, H. Yagi, and D. M. Jerlna, J. Am. Chem. SOC.,98,2973 (1976). (14)J. P. Glusker, H. L. Carrel, D. E. Zacha as, and R. G. Harvey, CancerBlochem. Biophys., 1, 43 (1974). (15)J. W. Daly, D. M. Jerina, and B. Witkop, Experientia, 28, 1129 (1972). (16)A. Pullman and 6. Pullman, "The Jerusalem Symposium on Quantum

Chemistry and Biochemistry",Vol. i, The Israel Academy of Science and Humanity,Jerusalem, 1967,p t4. (17)R. G. Harvey, S. H. Goh, and C. Cortez, J. Am. Chem. Soc., 97, 3468

(1975). (18)M. I. Kay, Y. Okaya, and D. E. Cox, Acta Crystallogr., Sect. 6, 27, 26 (1971). (19)J. lball and S. G. G. MacDonald, 2.Kristallogr., Kristallogeom., Kristallphys., Kristallchern., 114,439 (1960). (20)L. F. Fieser and M. Fieser, "Reagents for Organic Synthesis", Vol. 1, Wiley, New York, N.Y., 1966,p 333.